Disease #06669 (POF14 (?Premature ovarian failure 14), OMIM:618014)

Official abbreviation POF14
Name ?Premature ovarian failure 14
OMIM ID 618014
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GDF9
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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